Department of Civil, Architectural and Environmental Engineering, Missouri University of Science and Technology, Rolla, MO, United States of America.
Department of Mining and Nuclear Engineering, Missouri University of Science and Technology, Rolla, MO, United States of America.
PLoS One. 2020 Oct 30;15(10):e0241539. doi: 10.1371/journal.pone.0241539. eCollection 2020.
Particle size is an essential factor when considering the fate and transport of virus-containing droplets expelled by human, because it determines the deposition pattern in the human respiratory system and the evolution of droplets by evaporation and gravitational settling. However, the evolution of virus-containing droplets and the size-dependent viral load have not been studied in detail. The lack of this information leads to uncertainties in understanding the airborne transmission of respiratory diseases, such as the COVID-19. In this study, through a set of differential equations describing the evolution of respiratory droplets and by using the SARS-CoV-2 virus as an example, we investigated the distribution of airborne virus in human expelled particles from coughing and speaking. More specifically, by calculating the vertical distances traveled by the respiratory droplets, we examined the number of viruses that can remain airborne and the size of particles carrying these airborne viruses after different elapsed times. From a single cough, a person with a high viral load in respiratory fluid (2.35 × 109 copies per ml) may generate as many as 1.23 × 105 copies of viruses that can remain airborne after 10 seconds, compared to 386 copies of a normal patient (7.00 × 106 copies per ml). Masking, however, can effectively block around 94% of the viruses that may otherwise remain airborne after 10 seconds. Our study found that no clear size boundary exists between particles that can settle and can remain airborne. The results from this study challenge the conventional understanding of disease transmission routes through airborne and droplet mechanisms. We suggest that a complete understanding of the respiratory droplet evolution is essential and needed to identify the transmission mechanisms of respiratory diseases.
颗粒大小是考虑人类呼出含病毒飞沫的命运和传输的一个重要因素,因为它决定了飞沫在人体呼吸系统中的沉积模式以及飞沫通过蒸发和重力沉降的演变。然而,含病毒飞沫的演变以及与颗粒大小相关的病毒载量尚未得到详细研究。由于缺乏这些信息,导致人们对呼吸道疾病(如 COVID-19)的空气传播机制的理解存在不确定性。在这项研究中,我们通过一组描述呼吸飞沫演变的微分方程,并以 SARS-CoV-2 病毒为例,研究了咳嗽和说话时人类呼出飞沫中携带的病毒在空气中的分布。更具体地说,通过计算呼吸飞沫的垂直距离,我们研究了在不同的时间流逝后,能在空气中持续存在的病毒数量以及携带这些空气中病毒的颗粒大小。从单次咳嗽中,呼吸道液中病毒载量较高(2.35×109 拷贝/毫升)的人可能会产生多达 1.23×105 拷贝的病毒,这些病毒在 10 秒后仍能在空气中持续存在,而正常患者(7.00×106 拷贝/毫升)只有 386 拷贝。然而,口罩可以有效地阻挡 10 秒后可能仍在空气中持续存在的病毒的 94%左右。我们的研究发现,能沉降的颗粒和能在空气中持续存在的颗粒之间没有明显的大小界限。这项研究的结果挑战了通过空气传播和飞沫传播机制来理解疾病传播途径的传统观念。我们建议,全面了解呼吸飞沫的演变对于确定呼吸道疾病的传播机制至关重要。